A mechanism-based cleavage of lactam-carbamates
- 31 December 1994
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 35 (6) , 847-848
- https://doi.org/10.1016/s0040-4039(00)75979-x
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- A simple asymmetric synthesis of 2-substituted pyrrolidines and 5-substituted pyrrolidinonesThe Journal of Organic Chemistry, 1992
- Asymmetric synthesis of .gamma.,.gamma.-dialkyl-.gamma.-aminobutyric acid analogs and 2,2-disubstituted pyrrolidines. Control of stereochemistry in aminal ring opening by varying the extent of allylic 1,3 strainJournal of the American Chemical Society, 1991
- A simple asymmetric synthesis of 2-substituted pyrrolidines from 3-acylpropionic acidsThe Journal of Organic Chemistry, 1991
- Resolution of 4-Phenyl-2-pyrrolidinone: A Versatile Synthetic IntermediateSynthesis, 1991
- Selective inhibition of .gamma.-aminobutyric acid aminotransferase by (3R,4R), (3S,4S)- and (3R,4S), (3S,4R)-4-amino-5-fluoro-3-phenylpentanoic acidsJournal of Medicinal Chemistry, 1990
- A mild two-step method for the hydrolysis of lactams and secondary amidesThe Journal of Organic Chemistry, 1983